Next Article in Journal
Exploring the Antimicrobial Properties of 99 Natural Flavour and Fragrance Raw Materials against Pathogenic Bacteria: A Comparative Study with Antibiotics
Previous Article in Journal
Bio-Monitoring of Metal(loid)s Pollution in Dry Riverbeds Affected by Mining Activity
Previous Article in Special Issue
Multitask Approach to Localize Rhizobial Type Three Secretion System Effector Proteins Inside Eukaryotic Cells
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Plants
Volume 12
Issue 21
10.3390/plants12213776
plants-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Diverse Bradyrhizobium spp. with Similar Symbiosis Genes Nodulate Peanut in Different Regions of China: Characterization of Symbiovar sv. Arachis

by
Junjie Zhang
1,2,*,
Yufeng Feng
1,
Jingqi Wang
1,
Entao Wang
3 and
Mitchell Andrews
4,*
1
College of Food and Bioengineering, Zhengzhou University of Light Industry, Zhengzhou 450002, China
2
Collaborative Innovation Center for Food Production and Safety of Henan Province, Zhengzhou 450002, China
3
Departamento de Microbiología, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Ciudad de México 11340, Mexico
4
Faculty of Agriculture and Life Sciences, Lincoln University, Lincoln 7647, New Zealand
*
Authors to whom correspondence should be addressed.
Plants 2023, 12(21), 3776; https://doi.org/10.3390/plants12213776
Submission received: 9 October 2023 / Revised: 30 October 2023 / Accepted: 3 November 2023 / Published: 6 November 2023
(This article belongs to the Special Issue Molecular Mechanisms in Root Nodule Symbiosis)
Browse Figures
Versions Notes

Abstract

:
A total of 219 rhizobial strains isolated from peanut grown in soils from six peanut croplands in Zhengyang county, Henan Province, were typed by PCR-RFLP of IGS sequences. Their phylogenetic relationships were refined on representative strains using sequence analyses of 16S rRNA genes, housekeeping genes (atpD, recA, glnII) and symbiosis genes (nodA, nodC and nifH). The 219 rhizobial isolates were classified into 13 IGS types, and twenty representatives were defined within eight Bradyrhizobium genospecies: B. guangdongense covering 5 IGS types (75.2% of total isolates), B. guangzhouense (2 IGS types, 2.7% total isolates), B. zhengyangense (1 IGS type, 11.3% total isolates) and five novel genospecies (5 IGS types, 0.9 to 3.2% total isolates). All representative strains had identical nodA, nodC and nifH sequences except for one nifH sequence. With this one exception, these sequences were identical to those of the type strains of Bradyrhizobium species and several Bradyrhizobium genospecies isolated from peanut in different regions of China. The nodC sequences of all strains showed < 67% similarity to the closest strains on the Genbank database indicating that they are representative of a novel Bradyrhiobium symbiovar. This study has shown that (1) diverse Bradyrhizobium spp. with similar symbiosis genes nodulate peanut in different regions of China. (2) Horizontal transfer of genes involved in nodulating peanut is common between Bradyrhizobium species in soils used to grow the crop in China. (3) The strains studied here are representative of a novel Bradyrhizobium symbiovar that nodulates peanut in China. We propose the name sv. arachis for this novel symbiovar indicating that the strains were isolated from Arachis hypogaea. Results here have practical implications in relation to the selection of rhizobial inoculants for peanut in China.

1. Introduction

Legume species show specificity for rhizobial symbiont [1]. Mechanisms that maintain this specificity operate at different points in the nodulation process including during communication between the two organisms in the soil [2]. Generally, the nodulation process is initiated by the legume production of a mix of compounds, mainly flavonoids, into the rhizosphere. Different legume species produce different types and mixes of compounds that are specific to particular rhizobia. These compounds are absorbed by compatible rhizobia in the soil, and this activates their nodulation protein D (NodD) by stimulating the binding of NodD to nod gene promoters. The NodD protein triggers the transcription of a range of genes within the rhizobium including those required to produce Nod factors, the signal molecules from the rhizobium that induce nodule morphogenesis in the legume. These genes include nodABC that encode the enzymes required for the synthesis of the core Nod factor structure of an N-acetyl glucosamine oligosaccharide backbone with a fatty acyl chain at the non-reducing end. Nod factors differ in their length of the N-acetyl glucosamine oligosaccharide backbone and length and saturation of the fatty acid chain. Also, nod genes in addition to nodABC can encode species-specific substitutions to the Nod factor core. Specific nod genes, but nodC in particular, have been shown to be closely correlated with legume host specificity [3,4].
The symbiosis (sym) genes that enable rhizobial strains to induce N2-fixing nodules on legumes (nod, nif and fix genes) can be gained or lost as they are encoded on transferable plasmids or symbiosis islands. Horizontal transfer of sym genes can occur between, and more commonly within, bacterial genera [5,6]. Thus, strains of different rhizobial species within and across genera can have similar sym genes. Also, different strains within a particular rhizobial species can have different sym genes. The term symbiovar (sv.) describes strains of the same or different rhizobial species that are able to establish symbiosis with distinct legume species and can be distinguished by specific symbiotic gene phylogenies [3,4,7].
Cultivated peanut (Arachis hypogaea L.) originated and was domesticated in South America, but it is now an important grain and oil legume crop in many countries, with China the largest producer worldwide [8]. Often, crop legumes grown outside their normal range require inoculation with compatible rhizobia, but in China, peanut crops are not inoculated and rely on soil populations for nodulation. Previous studies in China reported peanut to be nodulated exclusively by Bradyrhizobium species and mainly native strains. Bradyrhizobium lablabi [9], B. arachidis [10], B. guangdongense, B. guangxiense, B. guangzhouense, B. nanningense, B. zhanjiangense [11,12] and B. zhengyangense [13] were isolated from peanut in different regions of China and formally described. Henan Province in central China has become the largest area for peanut production in China, with over 1.47 million hectares. Zhang et al. [14] characterized 217 strains isolated from peanut grown in soils from six field sites in the Nanyang city, administrative area, Henan Province. Phylogenetic analysis of recA, atpD and glnII genes of representative strains identified B. guangdongense, B. ottowaense and three novel Bradyrhizobium genospecies. Attempts to sequence the nodC gene of the isolates were unsuccessful. However, their nodA and nifH gene sequences were not congruent with the core genes on phylogenetic analysis and most strains showed sequences similar to those of Bradyrhizobium spp. isolated from peanut in southeast China. This indicates that horizontal transfer of nodA and nifH genes occurred between Bradyrhizobium in soils of peanut crops.
In the current study, the diversity of rhizobia-nodulating peanut in Henan Province was explored further. A total of 219 rhizobial strains isolated from peanut grown in soils from six peanut croplands in Zhengyang county were typed by PCR-RFLP of IGS sequences. Their phylogenetic relationships were refined on representative strains using sequence analyses of 16S rRNA genes, housekeeping genes (atpD, recA, glnII) and symbiosis genes (nodA, nodC and nifH). A new symbiovar of peanut is described.

2. Results

2.1. PCR-Based RFLP Analysis of IGS

A total of 219 peanut rhizobial strains were isolated in this study that separated into 13 IGS types (Table 1). IGS type 2 was the most prevalent with a total of 155 strains representing 69.82% of all isolates and occurred in all sites. IGS type 1 also occurred in all sites, with a total of 25 strains representing 11.26% of all isolates (Table 1). The remaining 11 IGS types occurred at one (IGS Types 6, 7, 9–13) or two (IGS types 3–5 and 8) sites. The number of different IGS types detected at each site varied from 2 (site ZD) to 8 (site ZA).

2.2. Phylogenetic Analysis of 16S rRNA and Housekeeping Genes

In 16S rRNA gene phylogeny, the 20 representative isolates formed a single and well-supported clade (97% bootstrap value) together with the type strains of 44 defined Bradyrhizobium species (Figure 1). The isolates separated into three subclades within this clade. Seventeen isolates showed identical or highly similar 16S rRNA sequences to B. guangdongense CCBAU 51649T and B. guangzhouense CCBAU 51670T isolated from peanut in Guangdong province, Southeast China [11,12], and B. manausense BR 3351T and B campsiandrae INPA 01-394BT (=UFLA 01-1174T) isolated from Vigna unguiculata and Campsiandra laurilifolia, respectively, in the Amazon region, Brazil [15,16]. Two isolates (WYCCWR 12671 and WYCCWR 12663) showed identical 16S rRNA sequences to B. ganzhouense RITF806T isolated from Acacia melanoxylon in Jiangxi Province, Southeast China [17]. The final strain (WYCCWR 12669) was most closely related to B. nitroreducens TSA1T isolated from rice paddy soil in Japan [18].
In the phylogeny of concatenated sequences of recA (350 bp), glnII (441 bp) and atpD (394 bp), the 20 representative strains formed eight clusters (genospecies) at a 97.0% similarity cut-off (Figure 2, Table 1). Similar grouping results were observed in the phylogenies for individual genes (Figures S1–S3). Cluster 1 (C1) contained ten representative strains of IGS types 2, 5, 9, 10 and 12, covering 167 isolates (75.2% of total isolates) that shared 98.5–100% concatenated sequence similarities with B. guangdongense CCBAU 51649T. Cluster 2 (C2) included the representative strains of IGS types 3 and 11 consisting of 6 isolates (2.7% of total), and their concatenated sequences showed 99.7% similarities with that of B. guangzhouense CCBAU 51670T. The three strains in Cluster 5, WYCCWR 13023T, WYCCWR 12678 and WYCCWR 12774 (IGS type 1) were formally described as a novel species B. zhengyangense in a separate study (13). Clusters 3 (IGS 13, 2 strains), 4 (IGS 4, 5 strains), 6 (IGS 8, 7 strains), 7 (IGS 7, 3 strains) and 8 (IGS 6, 4 strains) showed less than 96.7% similarities in MLSA with the defined Bradyrhizobium species. Based on these results, C1, C2 and C5 were affiliated to B. guangdongense, B. guangzhouense and B. zhengyangense, respectively, while clusters 3, 4, 6, 7 and 8 were considered as separate Bradyrhizobium genospecies.

2.3. Phylogenies of Symbiosis Genes

In the phylogenetic tree of the nodA gene, the 20 representative strains formed a unique branch together with B. guangdongense CCBAU 51649T and B. guangzhouense CCBAU 51670T isolated from peanut in Guangdong Province, southeast China, and B. guangxiense CCBAU 53363T isolated from peanut in Guangxi Province, south China [11,12] which showed 100% sequence (440 bp) similarities (Figure 3). In the nifH phylogenetic tree, all isolates except WYCCWR 12663 were identical to B. guangdongense CCBAU 51649T and B. guangzhouense CCBAU 51670T (Figure 4). Strain WYCCWR 12663 aligned closest to B. nitroreducens TSA1T (95.3% similarity) in the nifH phylogenetic tree. The nodC sequences of strains WYCCWR 13022, WYCCWR 12699 and WYCCWR 12677, three B. zhengyangense strains including WYCCWR 13023T, WYCCWR 12678 and WYCCWR 12774, B. guangxiense CCBAU 53363T, B. guangzhouense CCBAU 51670T and B. guangdongense CCBAU 51649T were identical and clearly separated from other Bradyrhizobium species (Figure 5 and Figure S4). The nodC sequences of all strains studied showed 66.0% and 63.2% similarity to B. neotropicale BR 10247T and B. macuxiense BR 10303T, respectively, the two closest related Bradyrhizobium type strains on nodC phylogeny (Figure 5).

3. Discussion

Zhang et al. [14] reported that 217 rhizobial isolates from peanut grown in soils from six field sites in Nanyang city administrative area, Henan province, central China, separated into eight IGS types. Phylogenetic analysis of recA, atpD and glnII genes of representative strains of these IGS types identified B. guangdongense, B. ottowaense and three novel Bradyrhizobium genospecies. In the current study, a collection of 219 rhizobial isolates from peanut grown in soils from six field sites in Zhengyang county, Henan province, identified 13 IGS types. Here, phylogenetic analysis of recA, atpD and glnII genes of representative strains identified B. guangdongense, B. guangzhouense and six genospecies in the genus Bradyrhizobium. Three strains of one of these genospecies were formally described as B. zhengyangense [13]. It is likely that at least some of the novel genospecies reported here and by Zhang et al. [14] are representative of other novel Bradyrhizobium spp., but further work is required to show that this is the case [13]. Data obtained in the current study are consistent with previous reports that in China, peanut is exclusively nodulated by Bradyrhizobium species and mainly native strains. They also show that peanut is nodulated by diverse Bradyrhizobium spp. in Henan province. This is also the case in Guangdong province, southeast China, another major area of peanut production [19]. Outside China, peanut is mainly, but not exclusively, nodulated by Bradyrhizobium spp. [1].
B. guangdongense was the most common isolate identified here and in the study of Zhang et al. [14]. This species is also a common rhizobial symbiont of peanut in soils of Guangdong province [11]. This finding of the same Bradyrhizobium peanut-nodulating species in Henan province and the distant Guangdong province could be related to the dispersion of cultivated peanut from southeast to central China. Shao et al. [20] found that B. liaoningense and B. ottawaense were the dominant peanut-nodulating species in Shandong Province that is adjacent to Henan Province. Therefore, biogeographic differences exist in the Bradyrhizobium peanut-nodulating species in China.
Zhang et al. [14] reported that the nodA and nifH gene sequences of peanut rhizobia from Henan province were not congruent with the core genes on phylogenetic analysis and most strains showed sequences similar to those of Bradyrhizobium spp. isolated from peanut in south/ southeast China. In particular, the nodA gene sequences of seven of the 11 representative strains of the eight IGS types assigned to B. guangdongense and Bradyrhizobium genospecies 2 and 3 were identical to those of B. guangdongense CCBAU 51649T, B. guangxiense CCBAU 53363T and B. guangzhouense CCBAU 51670T, all of which were isolated from peanut in south/southeast China [11,12]. The nifH sequences for these seven strains were identical to those of B. guangdongense CCBAU 51649T and B. guangzhouense CCBAU 51670T. Similarly, in the current study, the nodA gene sequences of the 20 representative strains formed a unique branch together with B. guangdongense CCBAU 51649T, B. guangzhouense CCBAU 51670T and B. guangxiense CCBAU 53363T which showed 100% sequence (440 bp) similarities and in the nifH phylogenetic tree, all isolates except WYCCWR 12663, were identical to B. guangdongense CCBAU 51649T and B. guangzhouense CCBAU 51670T. Also, the nodC sequences of strains WYCCWR 13022, WYCCWR 12699 and WYCCWR 12677, three B. zhengyangense strains including WYCCWR 13023T, WYCCWR 12678 and WYCCWR 12774, B. guangxiense CCBAU 53363T, B. guangzhouense CCBAU 51670T and B. guangdongense CCBAU 51649T were identical and clearly separated from other Bradyrhizobium species (Figure 5 and Figure S4). This indicates that horizontal transfer of nodA, nodC and nifH genes involved in nodulating peanut is common between Bradyrhizobium species in soils used to grow the crop in China [5,6].
The term symbiovar describes a group of rhizobial strains supported by similar phylogeny of symbiosis genes and host range. The current study and that of Zhang et al. [14] show that four formally described Bradyrhizobium species (B guangdongense CCBAU 51649T, B. guangxiense CCBAU 53363T, B. guangzhouense CCBAU 51670T and B. zhengyangense WYCCWR 13023T) and seven Bradyrhizobium genospecies have similar nodA, nodC and nifH gene phylogenies. Host range was not tested in either study. However, B guangdongense CCBAU 51649T, B. guangxiense CCBAU 53363T, B. guangzhouense CCBAU 51670T and B. zhengyangense WYCCWR 13023T show a similar host range in that they produce functional nodules on peanut and Lablab purpureus, either do not nodulate or produce ineffective nodules on Phaseolus vulgaris and Glycine max, and do not nodulate Medicago sativa, Trifolium repens and Vigna radiata [11,12,13] (unpublished data). Thus, phylogeny of symbiosis genes and host range of associated type strains indicate that the strains studied here represent a new symbiovar of Bradyrhizobium that nodulates peanut in China. Delamuta et al. [3] proposed that a similarity of nodC gene sequences of approximately 92.5% or less could be used for defining new symbiovars. Here, the nodC gene sequences of all strains tested in the current study showed <70% similarity to the closest strains on nodC phylogeny indicating a novel Bradyrhizobium symbiovar that nodulates peanut in China.
In summary, this study has shown that (1) diverse Bradyrhizobium spp. with similar symbiosis genes nodulate peanut in different regions of China. (2) Horizontal transfer of genes involved in nodulating peanut is common between Bradyrhizobium species in soils used to grow the crop in China. (3) The strains studied here are representative of a novel Bradyrhizobium symbiovar that nodulates peanut in China. We propose the name sv. arachis for this novel symbiovar indicating that the strains were isolated from peanut, Arachis hypogaea. The findings here have practical implications in relation to the selection of rhizobial inoculants for peanut in China. As a first step, further work will determine if the different genospecies studied here are adapted to and are more competitive in specific soils/soil conditions with the objective of producing specific peanut Bradyrhizobium inoculants for particular soil types.

4. Materials and Methods

4.1. Soil Sampling and Physicochemical Characterization

Soil samples were collected from six peanut croplands where the peanut variety Yuanza 9102 is frequently cultivated, in Zhengyang County (N32°22′23″–N32°40′52″, E114°18′59″–E114°29′30″), Henan province, central China. The sampling sites covered four soil types: fluvo-aquic soil, paddy soil, Shajiang black soil and yellow cinnamon soil. In all sites, peanut had been repeatedly cropped over a period extending from June to September for more than two decades, in rotation with winter wheat (Triticum aestivum L.) each year, except at site ZB, where a two-year rotation consisting of peanut/wheat and green manure (Astragalus sinicus L.)/rice (Oryza sativa L.) was applied. No rhizobial inoculation was carried out in the studied fields, as is the case for the whole of Zhengyang County. Soils were collected at a depth of 10 to 20 cm from each site, during the peanut full-bloom stage in August 2019. At each sampling site, five randomly selected subsamples were equally mixed in situ to constitute a composite sample and then transported to the laboratory in a surface-sterilized ice box. Climate data at the sampling sites were acquired from the DIVA-GIS database (http://www.diva-gis.org). Location, soil type, climate factors and cropping rotation system of each sampling site are shown in Table S1.
In the laboratory, soil samples were stored at 4 °C, and a fraction of each soil composite sample was used for triplicate measurement of pH, organic matter (OM), total nitrogen (TN), available phosphorus (AP), available potassium (AK) and total salts (TS) as reported previously [21,22]. The six soil samples had 11.9–21.1 g kg−1 OM, 0.83–1.27 g kg−1 TN, 18.1–62.5 mg kg−1 AP, 78.0–106 mg kg−1 AK, 1.07 to 1.77 g kg−1 TS and 4.8 to 6.2 pH (Table S2).

4.2. Rhizobial Isolation and Nodulation Test

For rhizobia trapping, soil samples were mixed with sterilized vermiculite (1/5, v/v) in surface-sterilized plastic pots (15 cm height × 10 cm diameter) and moistened with nitrogen-free plant nutrient solution containing CaSO4 0.46 g, KCl 0.075 g, MgSO4·7H2O 0.06 g, K2HPO4 0.136 g and FeC6H5O7 0.075 g in 1 L of pure water, supplemented with 1 mL of microelement solution containing ZnSO4 0.22 g, MnSO4 1.81 g, H3BO3 2.86 g, CuSO4·5H2O 0.8 g and H2MoO4 0.02 g per L of pure water. Peanut seeds of variety Yuanza 9102 purchased from Henan Academy of Agricultural Sciences were surface sterilized by immersing in 95% (v/v) ethanol for 30 s, followed by 2.5% (w/v) NaClO solution for 5 min, and then washed 8 times with sterilized water. After surface sterilization, seeds were transferred onto 0.5% water–agar in the dark at 25 °C for germination. One seedling with a root length of approximately 1 cm was sown in each pot and grown in a greenhouse for 45 days. Then, ten peanut plants were randomly uprooted from the pots of each soil sample, and four healthy mature nodules (red color inside indicating the presence of leghemoglobin) were randomly selected per plant, resulting in a total of forty nodules per soil sample (site).
Nodules obtained by plant trapping were sterilized as described above for seeds, and rhizobia were isolated by streaking crushed nodules on yeast extract mannitol agar (YMA) [23] plates followed by incubation at 28 °C for 7−14 days. A single colony from each nodule was purified by repeated streaking on YMA plates, and all purified isolates were maintained on plates at 4 °C for temporary storage and in YM broth containing 20% (w/v) glycerol at −80 °C for long term storage. Nodulation ability was tested for all isolates by inoculating each of them on peanut seedlings grown in vermiculite according to the procedures of Wei et al. [24,25]. The inoculant of each isolate was prepared as a two-day culture in 5 mL YM broth at 28 °C under rotary agitation (120 rpm) until OD600 = 0.8−1.0, and the inoculation dose was 0.1 mL (107−108 cells) of the culture per germinated seed. Seedlings inoculated with YM broth without bacteria were included as negative controls. Seed surface sterilization, germination, cultivation, and nodule observation were as described in the trapping experiment. All isolates were authenticated as rhizobia by their ability to induce mature healthy nodules on peanut (none of the control plants nodulated) and give greater total plant dry weight than the controls.

4.3. PCR-Based RFLP of 16S-23S rRNA Intergenic Spacer (IGS)

Genomic DNA of each rhizobial isolate was extracted according to Terefework et al. [26] and used as the template for PCR amplification of the intergenic spacer (IGS) region with primers IGS1490 (forward) and IGS132′ (reverse) [27]. Restriction fragment length polymorphism (RFLP) of the IGS-PCR products (approximately 900 bp) was performed by digesting a 5 µL aliquot separately with each of the restriction endonucleases HaeIII, MspI or AluI. Restriction fragments were separated by electrophoresis in an agarose gel (2.5%, w/v) [28] containing GoldView type I nucleotide dye (Solarbio, Beijing, China, Lot No. 20140820), and results were visualized and analyzed using the DNR Bio-Imaging System (MiniBIS Pro, Jerusalem, Israel). Isolates sharing the same restriction patterns were defined as the same IGS type, and grouping analysis of IGS types was performed as previously described using the UPGMA method [29].

4.4. Phylogenetic Analysis of 16S rRNA Genes

Randomly selected isolates representing the different IGS types were used for 16S rRNA gene amplification with primers P1 and P6 [27] from the DNA extracts described above. The PCR products were purified and sent for commercial sequencing (Sangon Biotech Company, Shanghai, China). The acquired sequences and related sequences obtained from the GenBank database (http://www.ncbi.nlm.nih.gov/blast/Blast.cgi (accessed on 26 September 2021)) with the BLAST program were aligned using the ClustalW program in the MEGA 7.0 package [30]. To estimate the phylogenetic relationships of the strains, the phylogenetic tree was reconstructed by the maximum-likelihood (ML) method using the best-fit nucleotide substitution model defined by the Model tool test after iteration [31]. The best-fit substitution model among the 24 models implemented in MEGA 7.0 was selected based on the lowest Bayesian Information Criterion (BIC). Tree stability was estimated by bootstrapping algorithms with 1000 replicates using the MEGA 7.0 software.

4.5. Phylogenetic Analyses of Housekeeping and Symbiosis Genes

For representative isolates, the housekeeping genes recA (recombination protein A), atpD (ATP synthase beta chain) and glnII (glutamine synthetase II) were independently amplified using the primer pairs recA41F/recA640R, atpD255F/atpD782R and glnII12F/glnII689R, respectively [32,33]. In addition, sequences of type strains sharing recA, atpD or glnII gene similarities greater than 90% with the new isolates were extracted from the NCBI database and retained to reconstruct phylogenetic trees. The symbiotic genes nodA (N-acyltransferase nodulation protein A) and nifH (nitrogenase iron protein) were amplified for all representative isolates with primer pairs nodA-1/nodA-2 [34] and nifHF/nifHR [35], respectively, under the corresponding PCR conditions.
All purified amplicons were commercially sequenced at Sangon Biotech Company (Shanghai, China) using the same primers as for PCR. The acquired and related sequences obtained from the GenBank database with the BLAST program, were aligned using the ClustalW program in MEGA 7.0 [30]. Model test was used to produce the best nucleotide substitution model for each alignment as described above. A maximum-likelihood phylogenetic tree with 1000 bootstrap replicates was reconstructed for each gene with the MEGA 7.0 software. The acquired sequences of recA, glnII and atpD from the isolates together with the corresponding gene sequences of the type strains for validated Bradyrhizobium species were manually concatenated and aligned using ClustalW. The concatenated gene tree was constructed with the ML method as described above.
An attempt was made to amplify the nodC (N-acetylglucosaminyl transferase nodulation protein C) gene of all representative isolates using the primer pairs nodCF/nodCI [35] and nodC540/nodC1160 [36], but this was unsuccessful. Instead, full genomes of selected strains were sequenced using Illumina HiSeq pair-end technology, assembled using SOAPdenovo and Falcon programs and annotated according to the NCBI Prokaryotic Genome Annotation Pipeline [37]. Complete sequences of the nodC genes were retrieved from the genomes of these strains deposited in the GenBank database of the National Center for Biotechnology Information (NCBI: www.ncbi.nlm.nih.gov), and they were aligned using the ClustalW program in MEGA 7.0 [30]. Model test was used to produce the best nucleotide substitution model for each alignment as described above. A maximum-likelihood phylogenetic tree with 1000 bootstrap replicates was reconstructed for each gene with the MEGA 7.0 software.

4.6. Genome Features

The genomes of the three novel strains were sequenced using Illumina HiSeq pair-end technology, assembled using SOAPdenovo and Falcon programs and annotated according to the NCBI Prokaryotic Genome Annotation Pipeline [37]. In this study, the whole genomes of WYCCWR 13022, WYCCWR 12699 and WYCCWR 12677 were deposited in NCBI with the accession numbers of JAUIZJ000000000, JAVTJN000000000 and JAUIZK000000000.

5. Conclusions

In conclusion, diverse Bradyrhizobium species with similar novel symbiosis genes nodulate peanut in different provinces in China. Horizontal transfer of genes involved in nodulating peanut is common between Bradyrhizobium species in soils used to grow the crop in China. A novel Bradyrhizobium symbiovar, sv. arachis, that nodulates peanut in China is described.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/plants12213776/s1, Figure S1. Maximum-likelihood phylogenetic tree based on recA gene sequences showing the relationships of rhizobia isolated from Arachis hypogaea L. from Zhengyang, Hennan Province. The tree was constructed under a T92+G+I model. Bootstrap confidence values >50% are indicated at the internodes. Bar = 5% nucleotide divergence. Figure S2. Maximum-likelihood phylogenetic tree based on glnII gene sequences showing the relationships of rhizobia isolated from Arachis hypogaea L. from Zhengyang, Hennan Province. The tree was constructed under a (TN93+G+I) model. Bootstrap confidence values >50% are indicated at the internodes. Bar = 2% nucleotide divergence. Figure S3. Maximum-likelihood phylogenetic tree based on atpD gene sequences showing the relationships of rhizobia isolated from Arachis hypogaea L. from Zhengyang, Hennan Province. The tree was constructed under a T92+G+I model. Bootstrap confidence values >50% are indicated at the internodes. Bar = 5% nucleotide divergence. Figure S4. Maximum-likelihood phylogenetic tree based on nodC gene full sequences showing the relationships of rhizobia isolated from Arachis hypogaea L. from Zhengyang, Hennan Province. The tree was constructed under a T92+G model. Bootstrap confidence values >50% are indicated at the internodes. Bar = 10% nucleotide divergence. The novel sv. arachis is suggested. Table S1. Soil sample sites in Zhengyang county, Zhumadian city, Henan Province and their pedo-climatic characteristics. Table S2. Comparison of the soil physicochemical characteristics in the different sampling sites. Values are average ± standard deviation of three sub-samples.

Author Contributions

Conceptualization and methodology, J.Z. and M.A.; software, J.Z.; validation, J.Z.; formal analysis and investigation, Y.F. and J.W.; writing—original draft preparation, J.Z.; writing—review and editing, J.Z., E.W. and M.A.; supervision, J.Z. and M.A.; project administration, J.Z.; funding acquisition, J.Z. and E.W. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by Central Plains youth top talent project (project no. Yuzutong [2023]No.11), the National Nature Science Foundation of China (project no. 31970006) and Henan University Science and Technology Innovation Talent Support Program (project no. 22HASTIT035) from J.Z. and the projects of Sabbatical Year and SIP20200726 authorized by IPN, Mexico from E.W.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

All the sequences of peanut-nodulating rhizobia in this study have been submitted to GenBank and are available with the accession numbers in Figures and Supplementary Figures.

Acknowledgments

We want to thank Hui Yu for the soil sampling from Zhengyang county, Henan Province.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Andrews, M.; Andrews, M.E. Specificity in legume-rhizobia symbioses. Int. J. Mol. Sci. 2017, 18, 705. [Google Scholar]
  2. Walker, L.; Lagunas, B.; Gifford, M.L. Determinants of host range specificity in legume-rhizobia symbiosis. Front. Microbiol. 2020, 11, 585749. [Google Scholar] [CrossRef] [PubMed]
  3. Delamuta, J.R.M.O.; Menna, P.; Ribeiro, R.A.; Hungria, M. Phylogenies of symbiotic genes of Bradyrhizobium symbionts of legumes of economic and environmental importance in Brazil support the definition of the new symbiovars pachyrhizi and sojae. Syst. Appl. Microbiol. 2017, 40, 254–265. [Google Scholar] [CrossRef] [PubMed]
  4. Klepa, M.S.; Helene, L.C.F.; Hara, G.O.; Hungria, M. Bradyrhizobium cenepequi sp. nov., Bradyrhizobium semiaridum sp. nov., Bradyrhizobium hereditatis sp. nov and Bradyrhizobium australafricanum sp. nov., symbionts of different leguminous plants of Western Australia and South Africa and definition of three novel symbiovars. Int. J. Syst. Evol. Microbiol. 2022, 72, 005446. [Google Scholar]
  5. Andrews, M.; De Meyer, S.; James, E.K.; Stepkowski, T.; Hodge, S.; Simon, M.F.; Young, J.P.W. Horizontal transfer of symbiosis genes within and between rhizobial genera: Occurrence and importance. Genes 2018, 9, 321. [Google Scholar] [CrossRef]
  6. Wardell, G.E.; Hynes, M.F.; Young, P.J.; Harrison, E. Why are rhizobial symbiosis genes mobile? Philos. Trans. R. Soc. B Biol. Sci. 2022, 377, 20200471. [Google Scholar] [CrossRef]
  7. Rogel, M.A.; Ormeño-Orrillo, E.; Romero, E.M. Symbiovars in rhizobia reflect bacterial adaptation to legumes. Syst. Appl. Microbiol. 2011, 34, 96–104. [Google Scholar] [CrossRef]
  8. FAO. Production Year Book; FAO: Rome, Italy, 2023. [Google Scholar]
  9. Chang, Y.L.; Wang, J.Y.; Wang, E.T.; Liu, H.C.; Sui, X.H.; Chen, W.X. Bradyrhizobium lablabi sp. nov., isolated from effective nodules of Lablab purpureus and Arachis hypogaea. Int. J. Syst. Evol. Microbiol. 2011, 61, 2496–2502. [Google Scholar] [CrossRef]
  10. Wang, R.; Chang, Y.L.; Zheng, W.T.; Zhang, D.; Zhang, X.X.; Sui, X.H.; Wang, E.T.; Hu, J.Q.; Zhang, L.Y.; Chen, W.X. Bradyrhizobium arachidis sp nov., isolated from effective nodules Arachis hypogaea grown in China. Syst. Appl. Microbiol. 2013, 36, 101–105. [Google Scholar] [CrossRef]
  11. Li, Y.H.; Wang, R.; Zhang, X.X.; Young, J.P.W.; Wang, E.T.; Sui, X.H.; Chen, W.X. Bradyrhizobium guangdongense sp. nov. and Bradyrhizobium guangxiense sp. nov., isolated from effective nodules of peanut. Int. J. Syst. Evol. Microbiol. 2015, 65, 4655. [Google Scholar] [CrossRef]
  12. Li, Y.H.; Wang, R.; Sui, X.H.; Wang, E.T.; Chen, W.X. Bradyrhizobium nanningense sp. nov., Bradyrhizobium guangzhouense sp. nov. and Bradyrhizobium zhanjiangense sp. nov., isolated from effective nodules of peanut in Southeast China. Syst. Appl. Microbiol. 2019, 42, 126002. [Google Scholar] [CrossRef] [PubMed]
  13. Zhang, J.; Wang, N.; Li, S.; Peng, S.; Andrews, M.; Zhang, X.; Zhang, Y.; Yu, H.; Song, J.; Chen, W.; et al. Bradyrhizobium zhengyangense sp. nov., isolated from effective nodules of Arachis hypogaea L. in central China. Int. J. Syst. Evol. Microbiol. 2023, 73, 005723. [Google Scholar]
  14. Zhang, J.J.; Peng, S.S.; Li, S.; Song, J.C.; Brunel, B.; Wang, E.T.; James, E.K.; Chen, W.F.; Andrews, M. Arachis hypogaea L. from acid soils of Nanyang (China) is frequently associated with Bradyrhizobium guangdongense and occasionally with Bradyrhizobium ottawaense or three Bradyrhizobium genospecies. Microb. Ecol. 2021, 84, 556–564. [Google Scholar] [CrossRef] [PubMed]
  15. Silva, F.V.; De Meyer, S.E.; Simoes-Araujo, J.L.; Barbe, T.D.C.; Xavier, G.R.; O″Hara, G.; Ardley, J.K.; Rumjanek, N.G.; Willems, A.; Zilli, J.E. Bradyrhizobium manausense sp. nov., isolated from effective nodules of Vigna unguiculata grown in Brazilian Amazonian rainforest soils. Int. J. Syst. Evol. Microbiol. 2014, 64, 2358–2363. [Google Scholar] [CrossRef] [PubMed]
  16. Michel, D.C.; Costa, E.M.D.; Guimares, A.A.; Carvalho, T.S.D.; Moreira, F.M.D.S. Bradyrhizobium campsiandrae sp. nov., a nitrogen-fixing bacterial strain isolated from a native leguminous tree from the Amazon adapted to flooded conditions. Arch. Microbiol. 2021, 203, 233–240. [Google Scholar] [CrossRef]
  17. Lu, J.K.; Dou, Y.J.; Zhu, Y.J.; Wang, S.K.; Sui, X.H.; Kang, L.H. Bradyrhizobium ganzhouense sp. nov., an effective symbiotic bacterium isolated from Acacia melanoxylon R. Br. nodules. Int. J. Syst. Evol. Microbiol. 2014, 64, 1900–1905. [Google Scholar] [CrossRef]
  18. Jang, J.; Ashida, N.; Kai, A.; Isobe, K.; Nishizawa, T.; Otsuka, S.; Yokota, A.; Senoo, K.; Ishii, S. Presence of Cu-type (NirK) and cd1-type (NirS) nitrite reductase genes in the denitrifying bacterium Bradyrhizobium nitroreducens sp. nov. Microbes Environ. 2018, 33, 326–331. [Google Scholar] [CrossRef]
  19. Chen, J.; Hu, M.; Ma, H.; Wang, Y.; Wang, E.T.; Zhou, Z.; Gu, J. Genetic diversity and distribution of bradyrhizobia nodulating peanut in acid-neutral soils in Guangdong Province. Syst. Appl. Microbiol. 2016, 39, 418–427. [Google Scholar] [CrossRef]
  20. Shao, S.; Chen, M.; Liu, W.; Hu, X.; Li, Y. Long-term monoculture reduces the symbiotic rhizobial biodiversity of peanut. Syst. Appl. Microbiol. 2020, 43, 126101. [Google Scholar] [CrossRef]
  21. AFNOR. Soil Quality, Determination of pH; AFNOR: Paris, France, 2005. [Google Scholar]
  22. Han, L.; Wang, E.; Han, T.; Liu, J.; Sui, X.; Chen, W.; Chen, W. Unique community structure and biogeography of soybean rhizobia in the saline-alkaline soils of Xinjiang, China. Plant Soil 2009, 324, 291–305. [Google Scholar] [CrossRef]
  23. Vincent, J.M. A Manual for the Practical Study of Root Nodule Bacteria; International Biological Programme (By) Blackwell Scientific: Oxford, UK, 1970; Volume 15, pp. 1–164. [Google Scholar]
  24. Wei, G.H.; Chen, W.M.; Zhu, W.F.; Chen, C.; Young, J.P.W.; Bontemps, C. Invasive Robinia pseudoacacia in China is nodulated by Mesorhizobium and Sinorhizobium species that share similar nodulation genes with native American symbionts. FEMS Microbiol. Ecol. 2009, 68, 320–328. [Google Scholar] [CrossRef]
  25. Zhang, J.J.; Shang, Y.M.; Wang, E.T.; Chen, W.F.; de Lajudie, P.; Li, B.Y.; Guo, C.; Yang, X.; Zheng, J.Q.; Liu, C.Z. Mesorhizobium jarvisii sv. astragali as predominant microsymbiont for Astragalus sinicus L. in acidic soils, Xinyang, China. Plant Soil 2018, 433, 201–212. [Google Scholar] [CrossRef]
  26. Terefework, Z.; Kaijalainen, S.; Lindstrom, K. AFLP fingerprinting as a tool to study the genetic diversity of Rhizobium galegae isolated from Galega orientalis and Galega officinalis. J. Biotechnol. 2001, 91, 169–180. [Google Scholar] [CrossRef] [PubMed]
  27. Laguerre, G.; Mavingui, P.; Allard, M.R.; Charnay, M.P.; Louvrier, P.; Mazurier, S.I.; Rigottier-Gois, L.; Amarger, N. Typing of rhizobia by PCR DNA fingerprinting and PCR-restriction fragment length polymorphism analysis of chromosomal and symbiotic gene regions: Application to Rhizobium leguminosarum and its different biovars. Appl. Environ. Microbiol. 1996, 62, 2029–2036. [Google Scholar] [CrossRef] [PubMed]
  28. Wang, E.T.; Van Berkum, P.; Sui, X.H.; Beyene, D.; Chen, W.X.; Martínez-Romero, E. Diversity of rhizobia associated with Amorpha fruticosa isolated from Chinese soils and description of Mesorhizobium amorphae sp. nov. Int. J. Syst. Bacteriol. 1999, 49, 51–65. [Google Scholar] [CrossRef]
  29. Vauterin, L.; Yang, P.; Hoste, B.; Pot, B.; Swings, J.; Kersters, K. Taxonomy of xanthomonads from cereals and grasses based on SDS-PAGE of proteins, fatty acid analysis and DNA hybridization. J. Gen. Microbiol. 1992, 138, 1467–1477. [Google Scholar] [CrossRef]
  30. Kumar, S.; Stecher, G.; Tamura, K. MEGA7: Molecular evolutionary genetics analysis version 7.0 for bigger datasets. Mol. Biol. Evol. 2015, 33, 1870–1874. [Google Scholar] [CrossRef] [PubMed]
  31. Posada, D.; Crandall, K.A. MODELTEST: Testing the model of DNA substitution. Bioinformatics 1998, 14, 817–818. [Google Scholar] [CrossRef]
  32. Vinuesa, P.; Silva, C.; Lorite, M.J.; Izaguirre-Mayoral, M.L.; Bedmar, E.J.; Martinez-Romero, E. Molecular systematics of rhizobia based on maximum likelihood and Bayesian phylogenies inferred from rrs, atpD, recA and nifH sequences, and their use in the classification of Sesbania microsymbionts from Venezuelan wetlands. Syst. Appl. Microbiol. 2005, 28, 702–716. [Google Scholar] [CrossRef]
  33. Vinuesa, P.; Silva, C.; Werner, D.; Martínez-Romero, E. Population genetics and phylogenetic inference in bacterial molecular systematics: The roles of migration and recombination in Bradyrhizobium species cohesion and delineation. Mol. Phylogenet. Evol. 2005, 34, 29–54. [Google Scholar] [CrossRef]
  34. Haukka, K.; Lindstrom, K.; Young, J.P. Three phylogenetic groups of nodA and nifH genes in Sinorhizobium and Mesorhizobium isolates from leguminous trees growing in Africa and Latin America. Appl. Environ. Microbiol. 1998, 64, 419–426. [Google Scholar] [CrossRef] [PubMed]
  35. Laguerre, G.; Nour, S.M.; Macheret, V.; Sanjuan, J.; Drouin, P.; Amarger, N. Classification of rhizobia based on nodC and nifH gene analysis reveals a close phylogenetic relationship among Phaseolus vulgaris symbionts. Microbiology 2001, 147, 981–993. [Google Scholar] [CrossRef] [PubMed]
  36. Sarita, S.; Sharma, P.K.; Priefer, U.B.; Prell, J. Direct amplification of rhizobial nodC sequences from soil total DNA and comparison to nodC diversity of root nodule isolates. FEMS Microbiol. Ecol. 2010, 54, 1–11. [Google Scholar] [CrossRef] [PubMed]
  37. Tatiana, T.; Michael, D.C.; Azat, B.; Vyacheslav, C.; Nawrocki, E.P.; Leonid, Z.; Alexandre, L.; Pruitt, K.D.; Mark, B.; James, O. NCBI prokaryotic genome annotation pipeline. Nucleic Acids Res. 2016, 44, 6614–6624. [Google Scholar]
Plants 12 03776 g001
Figure 1. Maximum-likelihood phylogenetic tree based on 16S rRNA gene sequences showing the relationships of rhizobia isolated from Arachis hypogaea L. grown in soil from Zhengyang, Henan Province. The tree was constructed under a T92+G model. Bootstrap confidence values > 50% are indicated at the internodes. Bar = 1% nucleotide divergence. GenBank accession numbers are shown in brackets. The bold strains are the representatives of the isolates in this study.
Figure 1. Maximum-likelihood phylogenetic tree based on 16S rRNA gene sequences showing the relationships of rhizobia isolated from Arachis hypogaea L. grown in soil from Zhengyang, Henan Province. The tree was constructed under a T92+G model. Bootstrap confidence values > 50% are indicated at the internodes. Bar = 1% nucleotide divergence. GenBank accession numbers are shown in brackets. The bold strains are the representatives of the isolates in this study.
Plants 12 03776 g001
Plants 12 03776 g002
Figure 2. Maximum-likelihood phylogenetic tree based on concatenated recA-glnII-atpD gene sequences showing the relationships of rhizobia isolated from Arachis hypogaea L. grown in soil from Zhengyang, Henan Province. The tree was constructed under a GTR+G+I model. Bootstrap confidence values >50% are indicated at the internodes. Bar = 5% nucleotide divergence. The bold strains are the representatives of the isolates in this study.
Figure 2. Maximum-likelihood phylogenetic tree based on concatenated recA-glnII-atpD gene sequences showing the relationships of rhizobia isolated from Arachis hypogaea L. grown in soil from Zhengyang, Henan Province. The tree was constructed under a GTR+G+I model. Bootstrap confidence values >50% are indicated at the internodes. Bar = 5% nucleotide divergence. The bold strains are the representatives of the isolates in this study.
Plants 12 03776 g002
Plants 12 03776 g003
Figure 3. Maximum-likelihood phylogenetic tree based on nodA gene sequences showing the relationships of rhizobia isolated from Arachis hypogaea L. grown in soil from Zhengyang, Henan Province. The tree was constructed using the T92+I model. Bootstrap confidence values > 50% are indicated at the internodes. Bar = 5% nucleotide divergence. The bold strains are the representatives of the isolates in this study.
Figure 3. Maximum-likelihood phylogenetic tree based on nodA gene sequences showing the relationships of rhizobia isolated from Arachis hypogaea L. grown in soil from Zhengyang, Henan Province. The tree was constructed using the T92+I model. Bootstrap confidence values > 50% are indicated at the internodes. Bar = 5% nucleotide divergence. The bold strains are the representatives of the isolates in this study.
Plants 12 03776 g003
Plants 12 03776 g004
Figure 4. Maximum-likelihood phylogenetic tree based on nifH gene sequences showing the relationships of rhizobia isolated from Arachis hypogaea L. grown in soil from Zhengyang, Hennan Province. The tree was constructed using the T92+G model. Bootstrap confidence values >70% are indicated at the internodes. Bar = 5% nucleotide divergence. The bold strains are the representatives of the isolates in this study.
Figure 4. Maximum-likelihood phylogenetic tree based on nifH gene sequences showing the relationships of rhizobia isolated from Arachis hypogaea L. grown in soil from Zhengyang, Hennan Province. The tree was constructed using the T92+G model. Bootstrap confidence values >70% are indicated at the internodes. Bar = 5% nucleotide divergence. The bold strains are the representatives of the isolates in this study.
Plants 12 03776 g004
Plants 12 03776 g005
Figure 5. Maximum-likelihood phylogenetic tree based on nodC gene sequences showing the relationships of rhizobia isolated from Arachis hypogaea L. grown in soil from Zhengyang, Henan Province. The tree was constructed using the T92+I model. Bootstrap confidence values > 50% are indicated at the internodes. Bar = 5% nucleotide divergence. Different symbiovars of Bradyrhizobium were analyzed in this tree and the novel sv. arachis is proposed.
Figure 5. Maximum-likelihood phylogenetic tree based on nodC gene sequences showing the relationships of rhizobia isolated from Arachis hypogaea L. grown in soil from Zhengyang, Henan Province. The tree was constructed using the T92+I model. Bootstrap confidence values > 50% are indicated at the internodes. Bar = 5% nucleotide divergence. Different symbiovars of Bradyrhizobium were analyzed in this tree and the novel sv. arachis is proposed.
Plants 12 03776 g005
Table 1. Identification of genomic species by MLSA and IGS type among Bradyrhizobium strains isolated from Arachis hypogaea grown in soil from Zhengyang, Henan Province.
Table 1. Identification of genomic species by MLSA and IGS type among Bradyrhizobium strains isolated from Arachis hypogaea grown in soil from Zhengyang, Henan Province.
Representative Isolate
WYCCWR no. (Field Site) 1		MLSA Similarity (%) with Species 3IGS TypeIsolate Number
(% of Total Isolates)
B.gdB.gzB.zhB.gxB.nnB.ar
Bradyrhizobium guangdongense (Cluster 1, C1) 2
13051 (ZC)98.794.693.693.594.094.12155 (69.82)
12658 (ZA)10093.194.493.794.194.2
13038 (ZB)98.794.693.693.594.094.1
13098 (ZD)98.794.693.693.594.094.1
12802 (ZE)10094.994.493.794.194.2
12718 (ZF)98.594.293.593.193.793.9
13015 (ZB)98.794.693.693.594.094.155 (2.25)
12803 (ZE)10094.994.493.794.194.293 (1.35)
13024 (ZB)98.594.293.593.193.793.9102 (0.90)
12807 (ZE)98.794.493.693.393.793.8122 (0.90)
Bradyrhizobium guangzhouense (C2)
12726 (ZF)94.999.795.094.294.193.734 (1.80)
12723 (ZF)94.999.795.094.294.193.7112 (0.90)
Bradyrhizobium genosp. I (C3)
12663 (ZA)95.496.796.094.994.994.2132 (0.90)
Bradyrhizobium genosp. II (C4)
12677 (ZA)94.594.994.994.094.294.245 (2.25)
Bradyrhizobium zhengyangense (C5)
13023 (ZB)94.494.910094.994.294.5125 (11.26)
12678 (ZA)94.595.099.794.994.394.5
12774 (ZE)94.595.199.795.194.494.7
Bradyrhizobium genosp. III (C6)
13022 (ZB)93.694.993.793.793.694.487 (3.15)
Bradyrhizobium genosp. IV (C7)
12671 (ZA)92.194.092.492.292.493.073 (1.35)
Bradyrhizobium genosp. V (C8)
12669 (ZA)92.894.994.094.493.294.764 (1.80)
1 ZA, Zhouwan, Dougou, Zhengyang county; ZB, Zhouwan, Dougou, Zhengyang county (Paddy soil); ZC, Dayu, Lanqing, Zhengyang county; ZD, Wanglaozhuang, Lanqing, Zhengyang county; ZE, Silou, Yongxing, Zhengyang county; ZF, Zhangzhai, Fuzhai, Zhengyang county; 2 Cluster or genomic species deduced from MLSA (concatenated recA-atpD-glnII) similarity values; 3 MLSA (concatenated recA-glnII-atpD) similarity values with the most closely related strains: B.gd, Bradyrhizobium guangdongense CCBAU 51649T; B.gz, Bradyrhizobium guangzhouense CCBAU 51670; B.zh, Bradyrhizobium. zhengyangense WYCCWR 13023T; B.gx, Bradyrhizobium. guangxiense CCBAU 53363T; B.nn, Bradyrhizobium nanningense CCBAU 53390T; B.ar, Bradyrhizobium arachidis CCBAU 051107T.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Zhang, J.; Feng, Y.; Wang, J.; Wang, E.; Andrews, M. Diverse Bradyrhizobium spp. with Similar Symbiosis Genes Nodulate Peanut in Different Regions of China: Characterization of Symbiovar sv. Arachis. Plants 2023, 12, 3776. https://doi.org/10.3390/plants12213776

AMA Style

Zhang J, Feng Y, Wang J, Wang E, Andrews M. Diverse Bradyrhizobium spp. with Similar Symbiosis Genes Nodulate Peanut in Different Regions of China: Characterization of Symbiovar sv. Arachis. Plants. 2023; 12(21):3776. https://doi.org/10.3390/plants12213776

Chicago/Turabian Style

Zhang, Junjie, Yufeng Feng, Jingqi Wang, Entao Wang, and Mitchell Andrews. 2023. "Diverse Bradyrhizobium spp. with Similar Symbiosis Genes Nodulate Peanut in Different Regions of China: Characterization of Symbiovar sv. Arachis" Plants 12, no. 21: 3776. https://doi.org/10.3390/plants12213776

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop